Disease #05861 (NEDSWMA;CPSQ1 (neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities (CPSQ1)), OMIM:619026)

Official abbreviation NEDSWMA;CPSQ1
Name neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities (CPSQ1)
OMIM ID 619026
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene HPDL
Associated tissues -
Disease features -
Remarks -
Date created 2020-10-23 08:54:34 +02:00 (CEST)
Date last edited 2023-12-06 12:38:41 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00373536 iw028 - - M no China Chinese - - - - NEDSWMA;CPSQ1 HP:0002353; HP:0002539; HP:0002079; HP:0003155; HP:0012704; HP:0001263; HP:0001250; HP:0001276 HPDL HPDL 2 2 Wenjuan Qiu
00373800 iw031 - - M no China chinese - - - - NEDSWMA;CPSQ1 HP:0002353; HP:0002539; HP:0002079; HP:0003155; HP:0012704; HP:0001263; HP:0001250; HP:0001276 HPDL HPDL 2 2 Wenjuan Qiu
00383056 - - - M no (Latvia) - - - - - NEDSWMA;CPSQ1 - HPDL HPDL 1 2 Baiba Lace
00438282 273560 - - F no Germany - - - - - NEDSWMA;CPSQ1 Intellectual disability, Heterotropia, Seizure, Secondary microcephaly GABRA1, HPDL GABRA1, HPDL 3 1 Andreas Laner
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